Effect of Mg Doping on the Structural and Optical Properties of CdS Nanoparticles Synthesized by co-Precipitation Method

Cd1 – xMgxS (x = 0.00, 0.05, 0.10, 0.15 and 0.20) nanoparticles were synthesized by co-precipitation method for the first time. Compositional, morphological, structural and optical studies of the as prepared samples were carried out by X-ray diffraction (XRD), Energy dispersive analysis of X-rays (EDAX), Scanning electron microscopy (SEM), Diffuse reflectance spectroscopy (DRS) and Photoluminescence (PL) techniques. XRD studies revealed the structural phase transition from cubic to hexagonal and increase in the average grain size of the nanoparticles (lie in the range 1.4 nm to 2.8 nm) with increasing Mg content. EDAX spectra rules out the existence of impurities in the samples. Bandgap widening was observed in all the samples compared to bulk CdS (2.42 eV). Decrease in bandgap (3.02 eV to 2.54 eV), luminescence quenching and red shift of luminescence peak position were observed with increasing Mg in Cd1 – xMgxS. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/3028

Carbon nanotube-enhanced photoelectrochemical properties of metallo-octacarboxyphthalocyanines

The photoelectrochemistry of metallo-octacarboxyphthalocyanines (MOCPc, where M = Zn or Si(OH)2) integrated with MWCNTs for the development of dye-sensitized solar cells (DSSCs) is reported. The DSSC performance (obtained from the photo-chronoamperometric and photo-impedimetric data) decreased as ZnOCPc > (OH)2SiOCPc. The incorporation of the MWCNTs on the surface of the TiO2 film (MOCPc–MWCNT systems) gave higher photocurrent density than the bare MOCPc complexes. Also, from the EIS results, the MOCPc–MWCNT hybrids gave faster charge transport kinetics (approximately three times faster) compared to the bare MOCPc complexes. The electron lifetime was slightly longer (ca. 6 ms) at the ZnOCPc systems than at the (OH)2SiOCPc system (ca. 4 ms) meaning that the presence of the MWCNTs on the surface of the TiO2 film did not show any significant improvement on preventing charge recombination process